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CGS 15435是一种有效的血栓素(TxA2)合成酶抑制剂(IC50: 1 nM)。CGS 15435作用于 PGI2合成酶、环氧合酶和脂合酶比作用于血栓素合成酶选择性低得多。
CGS 15435是一种有效的血栓素(TxA2)合成酶抑制剂(IC50: 1 nM)。CGS 15435作用于 PGI2合成酶、环氧合酶和脂合酶比作用于血栓素合成酶选择性低得多。


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| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 580 | 现货 | |
| 5 mg | ¥ 1,400 | 现货 | |
| 10 mg | ¥ 1,960 | 现货 | |
| 25 mg | ¥ 2,890 | 现货 | |
| 50 mg | ¥ 3,920 | 现货 | |
| 100 mg | ¥ 5,200 | 现货 | |
| 200 mg | ¥ 6,880 | 现货 |
TargetMol的所有产品仅用作科学研究或药证申报,不能被用于人体,我们不向个人提供产品和服务。请您遵守承诺用途,不得违反法律法规规定用于任何其他用途。
该分子属于定制产品。TargetMol拥有优秀的合成团队,经验和能力,可以为您提供高性价比的产品。
如您有任何问题,欢迎咨询,我们将竭诚为您服务。| 产品描述 | CGS 15435 is a potent thromboxen (TxA2) synthetase inhibitor (IC50: 1 nM). CGS 15435 acts on PGI2 synthase, cyclooxygenase and liposynthase with much less selectivity than on thromboxin synthase. |
| 靶点活性 | TXA2:1 nM |
| 体外活性 | CGS 15435 inhibited the formation of PGE2 (IC50:1200 μM), PGI2 synthetase (IC50:90 μM) and 5-lipoxygenase (IC50:60 μM).[1] |
| 体内活性 | The effect of CGS 15435 was long lasting, as the increase of plasma TxB2 levels was prevented even 24 hours after the administration of CGS 15435. CGS 15435 inhibited the formation of TxB2 significantly at 4, 6, 12 and 24 h after administration. Administration of CGS 15435 0.25 or 24 h before arachidonic acid (AA) did not increase TxB2 in surviving animals (4/4 and 5/6, respectively). The final TxB2 level in CGS15435A(pretreatment for 0.25 and 24 h) groups was significantly lower than that in arachidonic acid (AA) and daxibon (pretreatment for 2 h) groups.[1] |
| 分子量 | 356.85 |
| 分子式 | C20H21ClN2O2 |
| CAS No. | 95853-92-2 |
| Smiles | C(CCCCC(O)=O)C1=C(N(C)C=2C1=CC(Cl)=CC2)C=3C=CC=NC3 |
| 密度 | no data available |
| 存储 | |||||||||||||||||||||
| 溶解度信息 | DMSO: 3.57 mg/mL (10 mM), Sonication is recommended. | ||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||
DMSO
该溶液配制表仅适用于固体产品。对于液体产品,请根据标明的浓度或密度计算稀释方案。 | |||||||||||||||||||||
对于不同动物的给药剂量换算,您也可以参考 更多